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. 2021 Jan 14;49(3):1364–1382. doi: 10.1093/nar/gkaa1283

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© The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 8. — The number of ChIP-seq datasets (out of 41 datasets used in the meta-analysis of Nguyen et al. (43)) with p53 peaks versus half-site conservation categories. The occupancy of p53 on fully-conserved REs (CC category) is significantly higher than on partially conserved or fully degenerate p53 sites. P values are marked as follows: P = 0.037 *, P 0.001 **, P < 0.0001 ***.

Inline graphic — The number of ChIP-seq datasets (out of 41 datasets used in the meta-analysis of Nguyen et al. (43)) with p53 peaks versus half-site conservation categories. The occupancy of p53 on fully-conserved REs (CC category) is significantly higher than on partially conserved or fully degenerate p53 sites. P values are marked as follows: P = 0.037 *, P 0.001 **, P < 0.0001 ***.